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CS-W001157 4
Total: USD 88.00

6-Bromo-2-methyl-2H-indazol-5-ol

  • CAS No. 1403767-25-8

  • Cat. No. CS-0055288
  • Molecule weight227.06
  • Purity≥96%
  • MDL No.None

*For research and further manufacturing use only, not for direct human use.

6-Bromo-2-methyl-2H-indazol-5-ol|CS-0055288

Structure of 1403767-25-8

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General Information

  • CAS No. 1403767-25-8
  • Cat. No. CS-0055288
  • Purity ≥96%
  • MDL No. None
  • Storage 4°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₇BrN₂O
  • Molecular Weight 227.06
  • Synonym(s) 6-Bromo-5-hydroxy-2-methyl-2H-indazole
  • SMILES OC1=CC2=CN(C)N=C2C=C1Br

Description

6-Bromo-2-methyl-2H-indazol-5-ol features a brominated indazolone core with a methyl group at the 2-position and a hydroxyl substituent at C5, enabling direct functionalization in cross-coupling reactions. This bench-stable scaffold integrates readily into bioactive molecule design, particularly in kinase inhibitor and medicinal chemistry applications.

Application

6-Bromo-2-methyl-2H-indazol-5-ol serves as a versatile building block for the synthesis of bioactive heterocycles, enabling direct functionalization at C5 via palladium-catalyzed cross-coupling. The phenolic hydroxyl group provides a handle for derivatization, while the bromide facilitates further diversification through standard coupling reactions. Bench-stable and compatible with common protecting group strategies, it functions effectively in medicinal chemistry campaigns targeting kinase inhibitors and CNS-active compounds.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H320-H335
Precautionary Statements : P261-P280-P302+P352

Quality Control

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Computational Chemistry Data

  • TPSA   38.05
  • LogP   2.0414
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   0

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